| Lafora's disease | A form of progressive myoclonus epilepsy beginning from age 6 to 19; characterised by generalised tonic-clonic seizures, resting and action myoclonus, ataxia, dementia, and classic EEG findings, including polyspike and wave discharges; basophilic cytoplasmic inclusion bodies present in portions of the brain, the liver, and skin, as well as the duct cells of the sweat glands. Death usually occurs within 10 years of onset; autosomal recessive inheritance. Synonym: Lafora's disease. (05 Mar 2000) |
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| Lafora body | An intraneural intracytoplasmic inclusion body composed of acid mucopolysaccharides, seen in familial myoclonus epilepsy; a recessive trait. (05 Mar 2000) |
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| Lafora body disease | A form of progressive myoclonus epilepsy beginning from age 6 to 19; characterised by generalised tonic-clonic seizures, resting and action myoclonus, ataxia, dementia, and classic EEG findings, including polyspike and wave discharges; basophilic cytoplasmic inclusion bodies present in portions of the brain, the liver, and skin, as well as the duct cells of the sweat glands. Death usually occurs within 10 years of onset; autosomal recessive inheritance. Synonym: Lafora's disease. (05 Mar 2000) |
| Lafora, Gonzalo Rodriguez | <person> Spanish neurologist, 1887-1971. See: Lafora body, Lafora body disease, Lafora's disease. (05 Mar 2000) |
| Lafora's disease |
myoclonus epilepsy: epilepsy characterized by clonus of muscle groups and progressive mental deterioration and genetic origin
출처: wordnet.princeton.edu/perl/webwn
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| Lafora's bodies |
intracytoplasmic inclusions consisting of a complex of glycoprotein and acid mucopolysaccharide; widespread deposits of these bodies are found in Lafora's myoclonus epilepsy.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| Lafora's sign |
picking of the nose regarded as an early sign of cerebrospinal meningitis.
출처: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
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| Lafora's disease |
A progressive myoclonic encephalopathy (PME) that is inherited as an autosomal recessive trait. Associated symptoms typically begin in childhood or early adolescence and include frequent seizures characterized by loss of consciousness and rhythmic contraction and relaxation of all muscle groups (generalized tonic-clonic seizures); sudden, involuntary, "shock-like" muscle jerks (myoclonus); and rapidly progressive deterioration of thought processing and acquired intellectual abilities ...
출처: www.dbs-stn.org/glossary2.asp
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| Lafora's bodies |
Cytoplasmic inclusion bodies made of acid mucopolysaccharides. They may be found in neuronal tissues taken from patients with familial myoclonic epilepsy.
출처:
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| lafora\'s | epilepsy characterized by clonus of muscle groups and progressive mental deterioration and genetic origin |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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